| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bae77f6f91bc37c3f3a6bab5b85a49fb |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6858 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6858
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 |
| filingDate |
2018-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_97c2ad372486b8f0298990f7e69fef39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_04081f6dd366871da04d998c0170c22a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc485ea0bde86f3a6552dd604854cc8e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b3ed1dad1f3c5f7645f1ee0a3f6bcbd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6df96f351d32cde3a8d605ce94a89425 |
| publicationDate |
2018-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
CN-108977518-A |
| titleOfInvention |
The detection method and detection kit in a kind of folic acid metabolism associated gene mutation site |
| abstract |
The invention discloses a kind of detection methods in folic acid metabolism associated gene mutation site, comprising the following steps: extracts sample DNA；Designed for expanding the specific primer of folic acid metabolism related gene segment；Target fragment is obtained using Single-tube multiplex-PCR amplified reaction；Single base extension primer designed for folic acid metabolism related gene segment；Folic acid metabolism related gene segment Single base extension；Nucleic acid mass spectral analysis measures target dna sequence, folic acid associated metabolic gene mutation for screening effectively can be unfolded to colorectal cancer patients, individual is helped to fully understand the hereditary conditions of oneself, carries out personalized precisely diagnosis and treatment for such patient and establishes clinical and scientific research basis.The invention further relates to a kind of detection kits in folic acid metabolism associated gene mutation site. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110438209-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110042158-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109988831-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110468184-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109880901-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110484609-A |
| priorityDate |
2018-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |